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Effect of Isoflurane Exposure with Administration of Polyunsaturated Fatty Acids on Cognition in Developing Rats
OBJECTIVE: The developing brain is vulnerable to the negative effects of anaesthetics. We aimed to investigate the effect of isoflurane and polyunsaturated fatty acids (PUFAs) on cognition. METHODS: A total of 64, ten days old rats were randomly divided into 4 groups: group O2 (oxygen group), group...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Turkish Anaesthesiology and Intensive Care Society
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7720831/ https://www.ncbi.nlm.nih.gov/pubmed/33313587 http://dx.doi.org/10.5152/TJAR.2020.128 |
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author | Aldemir Şensoy, Didem Demirgan, Serdar Akyol, Onat Gümüş Özcan, Funda Selcan, Ayşin |
author_facet | Aldemir Şensoy, Didem Demirgan, Serdar Akyol, Onat Gümüş Özcan, Funda Selcan, Ayşin |
author_sort | Aldemir Şensoy, Didem |
collection | PubMed |
description | OBJECTIVE: The developing brain is vulnerable to the negative effects of anaesthetics. We aimed to investigate the effect of isoflurane and polyunsaturated fatty acids (PUFAs) on cognition. METHODS: A total of 64, ten days old rats were randomly divided into 4 groups: group O2 (oxygen group), group Iso (isoflurane group), group Iso-S (isoflurane+saline) and group Iso-PUFAs (isoflurane+intraperitoneal [IP] PUFAs emulsion). Rats in groups Iso, Iso-S and Iso-PUFAs were exposed to 1.5% isoflurane in 50% oxygen for 6 hours. Rats in group O2 breathed only 50% oxygen. Before anaesthesia, rats in group Iso-S were administered 0.5 mL isotonic and rats in group Iso-PUFAs were administered 5 mL kg(−1) PUFAs emulsion by IP injection. The Morris water maze (MWM) test was performed on postnatal 28–33 days. Histological evaluation and immune histochemical staining (Bcl-2 antibody) were performed on postnatal day 11 on rat brains. RESULTS: As demonstrated by the reduction in the escape latency on days 3, 4 and 5 compared with day 1, all rats learned the task during the acquisition period. In contrast to others, rats in group Iso spent significantly lower time to find the platform on day 2 than on day 1 (p=0.034). No significant difference was found among the groups in terms of time spent in finding the platform. There were no significant differences in probe trials, histological features and Bcl-2 immunoreactivity among the groups. CONCLUSION: Isoflurane did not cause cognitive dysfunction and neuronal death, and a single dose of PUFAs emulsion had no effect on cognition either. |
format | Online Article Text |
id | pubmed-7720831 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Turkish Anaesthesiology and Intensive Care Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-77208312020-12-10 Effect of Isoflurane Exposure with Administration of Polyunsaturated Fatty Acids on Cognition in Developing Rats Aldemir Şensoy, Didem Demirgan, Serdar Akyol, Onat Gümüş Özcan, Funda Selcan, Ayşin Turk J Anaesthesiol Reanim Original Article OBJECTIVE: The developing brain is vulnerable to the negative effects of anaesthetics. We aimed to investigate the effect of isoflurane and polyunsaturated fatty acids (PUFAs) on cognition. METHODS: A total of 64, ten days old rats were randomly divided into 4 groups: group O2 (oxygen group), group Iso (isoflurane group), group Iso-S (isoflurane+saline) and group Iso-PUFAs (isoflurane+intraperitoneal [IP] PUFAs emulsion). Rats in groups Iso, Iso-S and Iso-PUFAs were exposed to 1.5% isoflurane in 50% oxygen for 6 hours. Rats in group O2 breathed only 50% oxygen. Before anaesthesia, rats in group Iso-S were administered 0.5 mL isotonic and rats in group Iso-PUFAs were administered 5 mL kg(−1) PUFAs emulsion by IP injection. The Morris water maze (MWM) test was performed on postnatal 28–33 days. Histological evaluation and immune histochemical staining (Bcl-2 antibody) were performed on postnatal day 11 on rat brains. RESULTS: As demonstrated by the reduction in the escape latency on days 3, 4 and 5 compared with day 1, all rats learned the task during the acquisition period. In contrast to others, rats in group Iso spent significantly lower time to find the platform on day 2 than on day 1 (p=0.034). No significant difference was found among the groups in terms of time spent in finding the platform. There were no significant differences in probe trials, histological features and Bcl-2 immunoreactivity among the groups. CONCLUSION: Isoflurane did not cause cognitive dysfunction and neuronal death, and a single dose of PUFAs emulsion had no effect on cognition either. Turkish Anaesthesiology and Intensive Care Society 2020-12 2020-12-01 /pmc/articles/PMC7720831/ /pubmed/33313587 http://dx.doi.org/10.5152/TJAR.2020.128 Text en © Copyright 2020 by Turkish Anaesthesiology and Intensive Care Society This work is licensed under Creative Common Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) ) |
spellingShingle | Original Article Aldemir Şensoy, Didem Demirgan, Serdar Akyol, Onat Gümüş Özcan, Funda Selcan, Ayşin Effect of Isoflurane Exposure with Administration of Polyunsaturated Fatty Acids on Cognition in Developing Rats |
title | Effect of Isoflurane Exposure with Administration of Polyunsaturated Fatty Acids on Cognition in Developing Rats |
title_full | Effect of Isoflurane Exposure with Administration of Polyunsaturated Fatty Acids on Cognition in Developing Rats |
title_fullStr | Effect of Isoflurane Exposure with Administration of Polyunsaturated Fatty Acids on Cognition in Developing Rats |
title_full_unstemmed | Effect of Isoflurane Exposure with Administration of Polyunsaturated Fatty Acids on Cognition in Developing Rats |
title_short | Effect of Isoflurane Exposure with Administration of Polyunsaturated Fatty Acids on Cognition in Developing Rats |
title_sort | effect of isoflurane exposure with administration of polyunsaturated fatty acids on cognition in developing rats |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7720831/ https://www.ncbi.nlm.nih.gov/pubmed/33313587 http://dx.doi.org/10.5152/TJAR.2020.128 |
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